Recent advances and future directions in the management of the immunocompromised host

Konrad Bochennek1, Marie Luckowitsch1, Thomas Lehrnbecher1

  • 1Division for Pediatric Hematology and Oncology, Hospital for Children and Adolescents, University Hospital, Goethe University Frankfurt am Main, Frankfurt, Germany.

Seminars in Oncology
|March 14, 2020
PubMed

Insights

Infectious complications pose significant risks for pediatric cancer patients. Personalized anti-infective strategies and improved diagnostics are crucial for better outcomes in children undergoing cancer therapy or stem cell transplantation.

Area of Science:

  • Pediatric Oncology
  • Infectious Diseases
  • Hematopoietic Stem Cell Transplantation

Background:

  • Infectious complications are a primary cause of morbidity and mortality in pediatric cancer patients and those undergoing hematopoietic stem cell transplantation (HSCT).
  • Current infection risk prediction models require refinement for personalized anti-infective strategies in this vulnerable population.
  • Diagnostic tool performance may vary between pediatric and adult patients, necessitating pediatric-specific assessments.

Purpose of the Study:

  • To highlight the need for improved risk-prediction models for infections in pediatric cancer patients.
  • To emphasize the importance of developing and validating pediatric-specific diagnostic tools for early and reliable infection detection.
  • To address the ongoing debate regarding the balance between benefits and risks of prophylactic anti-infective therapies in children.

Main Methods:

  • Review of current supportive care strategies and risk-prediction models in pediatric oncology and HSCT.
  • Analysis of the limitations of existing diagnostic tools in the pediatric population.
  • Discussion of the challenges and considerations in systemic antibacterial and antifungal prophylaxis.

Main Results:

  • Existing risk-prediction models for infections in pediatric cancer patients need refinement for personalization.
  • Pediatric-specific diagnostic tools and combinations require further assessment to improve early infection diagnosis.
  • The use of prophylactic antibacterial and antifungal agents presents a complex balance between reducing infections and increasing resistance.

Conclusions:

  • Significant research gaps remain in optimizing supportive anti-infective care for children undergoing cancer therapy or HSCT.
  • Development of pediatric-specific clinical practice guidelines has progressed, but further efforts are essential.
  • Personalized approaches to infection prevention and diagnosis are critical for improving outcomes in pediatric oncology and HSCT.

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